A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16266427



Internal ID20475645
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:24964830..24965508hg38UCSC Ensembl
chr4:24966452..24967130hg19UCSC Ensembl
Cytoband4p15.2
Allele length
AssemblyAllele length
hg38679
hg19679
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4747954
Supporting Variants
Samples
Known GenesCCDC149
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16266427
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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